Kraj: Irlandia
Język: angielski
Źródło: HPRA (Health Products Regulatory Authority)
Ivermectin
ECO Animal Health Europe Limited
QP54AA01
Ivermectin
0.5 percent
Pour-on solution
POM: Prescription Only Medicine as defined in relevant national legislation
ivermectin
Authorised
2001-05-17
1 NAME OF THE VETERINARY MEDICINAL PRODUCT Vetimec 5 mg/ml Pour-on Solution for Cattle 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each ml of solution contains: Active Substance Ivermectin 5 mg Excipients Benzyl Alcohol (as preservative) 10 mg For a full list of excipients, see section 6.1 3 PHARMACEUTICAL FORM Pour-on solution. 4 CLINICAL PARTICULARS 4.1 TARGET SPECIES Cattle. 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES In cattle: For the treatment of infections with the following parasites Gastro-intestinal worms - _Haemonchus placei _(adult and fourth stage larvae) _Ostertagia ostertagi _(adult and fourth stage larvae, including inhibited larvae) _Trichostrongylus axei _(adult and fourth stage larvae) _Trichostrongylus colubriformis _(adult and fourth stage larvae) _Cooperia punctata _(adult only) _Cooperia oncophora _(adult only) _Strongyloides papillosus _(adult only) _Oesophagostomum radiatum, _(adult and fourth stage larvae) Lungworm (adult and fourth stage larvae) – _Dictyocaulus viviparus_. Warbles (parasitic stages) – _Hypoderma bovis_, _Hypoderma lineatum_. Mange mites – _Sarcoptes scabiei var. bovis_. The product may also be used to reduce infection of the mange mite _Chorioptes bovis, _but complete elimination may not occur. Sucking and biting lice – _Linognathus vituli_, _Haematopinus eurysternus_, _Bovicola (Damalinia) bovis._ Ecomectin Cattle Pour-On has persistent activity against infections acquired with _Trichostrongylus axei _and _Cooperia spp. _up to 14 days after treatment, but only in the case of group treatment; _Ostertagia ostertagi _ and _Oesophagostomum radiatum _up to 21 days after treatment; _Dictyocaulus viviparus _up to 28 days after treatment. It also has persistent activity against horn flies (_Haematobia irritans_) for up to 28 days after treatment; partial efficacy against _Haematobia irritans _may last for up to 35 days post application. 4.3 CONTRAINDICATIONS Do not use in cases of known hypersensitivity to the active ingredient. Do not use in lactating dairy Przeczytaj cały dokument